- Regulatory Affairs Manager (m/w) Coagulation
Regulatory Manager, Development Products (m/w) Biotechnology Office-based in Switzerland, full-time Job Description: - Develop the Regulatory strategy for new and for licensed products in Europe for applications via centralized and national procedures (DCP, MRP). - Communicate and ensure the implementation of the European Regulatory strategy in global teams. ...
- Regulatory Manager, OTC
An exciting opportunity has arisen for an experienced Regulatory Affairs Manager to join one of the world's largest Pharmaceutical companies within their global OTC Regulatory team. You will be mainly focusing on new submissions on a global scale.
- QA/RA Manager-New Start Up Company-Medical Devices-St.Gallen
A new start up company specialising in innovative medical devices are looking for a regulatory affairs and quality manager. This is a fantastic role to build the QMS and regulatory function from scratch; allowing you to leave you market on this new exciting company. Be the key expert within qa/ra within this role and develop invaluable experience and autonomy.
- Great role in beautiful GHENT - RA Manager - Medical Devices - International role
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or email;firstname.lastname@example.org
- Key Account Manager – Paris – Antibiotics Launch
An opportunity with an expanding biopharmaceutical company has become available as a Key Account Manager, working specifically with a new antibiotic product that is due for launch within the coming months. This new antibiotic drug has already experienced incredible success in the USA and is now being launched across Europe, focusing specifically on countries such as France, Germany and the UK.
- Project Manager/Launch Facilitator, Global Projects
Due to continued growth Worldwide Clinical Trials (WCT) have a vacancy for a Launch Facilitator, Global Projects.
Permanant, Nottingham office based.
The Launch Facilitator will coordinate and lead the Launch of Late Phase Full Service Studies (i.e., those awards including Project Management and at least one other service).
- R E G U L A T O R Y CMC *** Large Molecule ** Lausanne Vevey area *** RA CMC Bio strategy for a P2B to P3 molecule ** Senior RA CMC Manager
This role is on exclusive assignment to Advanced Search & Selection. Please contact Theo Moore or Matt Greig initially on +44 20 7801 3380 or +44 7918 679 405 (until 9.00 pm CET and Saturday mornings) or send a full CV and contact information to email@example.com or firstname.lastname@example.org who will support your assessment and on boarding process.
- Senior Regulatory Affairs Manager (m/w)
Regulatory Affairs Manager (m/w)Office-based in BaselMy client is an international top-10 pharmaceutical and biotech company. For their EU headquarters in Basel, I am looking for an experienced Regulatory Affairs Manager to manage all regulatory activities (full lifecycle) for a specific therapeutic area. ...
- Global Regulatory Affairs Manager- Start-up, Zurich
Global Regulatory Affairs Manager- Start-up, Zurich Area, Fast paced atmosphere, Highly successful SMEExcellent opportunity to join a highly featured new player in the Pharmaceutical world who are expanding their EU regulatory team in preparation of major launches this year. In this position you will be involved in both hands on, commercial and strategic regulatory activities covering writing for CTD modules, variations/renewals as well as due diligence and health authority interactions. ...
- Senior Regulatory Affairs Associate/ RA
Vacancy: Senior Regulatory Affairs Associate/ Senior RA AssociateLocation: BerkshireSalary: £30,000- £40,000 per annumA Contract Research Organization (CRO) in Berkshire are currently looking for a Senior Regulatory Affairs Associate to join their team on a permanent basis.Senior Regulatory Affairs Associate: Key Responsibilities- Job Summary:
Compiles and submits clinical trial applications and notifications to regulatory authorities and ethics committees. ...